Fenwal, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fenwal, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Fenwal, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lake Zurich, US.
Historical record: 3 cleared submissions from 2008 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fenwal, Inc. Filter by specialty or product code using the sidebar.
Fenwal, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Jun 10, 2014
AMICUS SEPARATOR SYSTEM/ AMICUS SEPERATOR SYSTEM
Gastroenterology & Urology
50d
Cleared
Mar 22, 2012
AMICUS SEPARATOR SYSTEM- USE IN THERAPEUTIC PLASMA EXCHANGE AND FILTER SET...
Gastroenterology & Urology
279d
Cleared
Mar 03, 2008
BLOOD COMPONENT RECIPIENT SET WITH STANDARD SIZE FILTER AND INFUSION SET WITH...
General Hospital
96d